Identify the product of the following reaction:
Identify the product of the following reaction:
Benzene diazonium halide
Nitro benzene
Sodium benzoate
Benzene halide
The Correct Option is A
Solution and Explanation
The correct option is (A): Benzene diazonium halide
Top Questions on Organic Chemistry- Some Basic Principles and Techniques
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List-I
(Conversion)List-II
(Shape/geometry)(A) 1 mol of H2O to O2 (I) 3F (B) 1 mol of MnO-4 to Mn2+ (II) 2F (C) 1.5 mol of Ca from molten CaCl2 (III) 1F (D) 1 mol of FeO to Fe2O3 (IV) 5F
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Statement II : When branching increases, the molecule attains a shape of sphere. This results in smaller surface area for contact, due to which the intermolecular forces between the spherical molecules are weak, thereby lowering the boiling point.
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(Complex)List-II
(Type of isomerism)(A) [Co(NH3)5(NO2)]Cl2 (I) Solvate isomerism (B) [Co(NH3)5(SO4)]Br (II) Linkage isomerism (C) [Co(NH3)6] [Cr(CN)6] (III) Ionization isomerism (D) [Co(H2O)6]Cl3 (IV) Coordination isomerism
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Concepts Used:
Organic Chemistry – Some Basic Principles and Techniques - Reaction Mechanism
SN1 Reaction Mechanism:
SN1 reaction mechanism takes place by following three steps –
- Formation of carbocation
- Attack of nucleophile
- Deprotonation
SN2 Reaction Mechanism:
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
Electrophilic Aromatic Substitution Reaction Mechanism:
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
- A new sigma bond from C=C is formed during the reaction in the arene nucleophile.
- Due to the breaking of the C-H sigma bond, a proton is removed.
- The C=C bond is reformed and it restores the aromaticity of the compound.
Electrophilic Substitution Reaction Mechanism:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.
- Electrophile Generation
- Carbocation Formation
- Proton Removal